Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Katie M. Saulnier"'
Autor:
Stephanie O. M. Dyke, Katie M. Saulnier, Charles Dupras, Amy P. Webster, Karen Maschke, Mark Rothstein, Reiner Siebert, Jörn Walter, Stephan Beck, Tomi Pastinen, Yann Joly
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-9 (2019)
Abstract As epigenetic studies become more common and lead to new insights into health and disease, the return of individual epigenetic results to research participants, in particular in large-scale epigenomic studies, will be of growing importance.
Externí odkaz:
https://doaj.org/article/3fcc58747b254ada85d411965fa7bf4e
Publikováno v:
FACETS, Vol 1, Pp 138-147 (2016)
In setting up a data access policy to share controlled access data from the McGill Epigenomics Mapping Centre (EMC), an International Human Epigenome Consortium (IHEC) partner project, we encountered ethical and legal challenges that are likely to be
Externí odkaz:
https://doaj.org/article/f003f5ca0905489b875d90e1fee358b6
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Over more than two decades, various policies have been adopted worldwide to restrict the use of individual genetic information for non-medical reasons by third parties and prevent ‘genetic discrimination’. In this paper, we bring attention to the
Externí odkaz:
https://doaj.org/article/b53d93478fd94cc38dbf8509e4f67bcb
Publikováno v:
Social Studies of Science
Epigenetics, defined as ‘the study of mitotically and/or meiotically heritable changes in gene function that cannot be explained by changes in DNA sequence’, has emerged as a promissory yet controversial field of scientific inquiry over the past
Autor:
Jörn Walter, Mark A. Rothstein, Karen J. Maschke, Reiner Siebert, Tomi Pastinen, Yann Joly, Stephan Beck, Charles Dupras, Stephanie O.M. Dyke, Amy P. Webster, Katie M. Saulnier
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-9 (2019)
Genome Medicine
Genome Medicine
As epigenetic studies become more common and lead to new insights into health and disease, the return of individual epigenetic results to research participants, in particular in large-scale epigenomic studies, will be of growing importance. Members o
Autor:
Obiajulu Nnamuchi, Bartha Maria Knoppers, Alexandra Obadia, Katie M. Saulnier, Mark A. Rothstein, Heather L. Harrell, Gil Siegal, Tzu-Hsun Hung, Chien-Te Fan, Edward S. Dove
Publikováno v:
IRB: Ethics & Human Research. 40:7-12
Publikováno v:
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC. 43(3)
Intersex individuals face human rights violations, discrimination, and stigmatization worldwide. Diagnosis in infants is uncommon, with between 1 in 2000 and 1 in 4500 infants born with ambiguous external genitalia sufficient to warrant genetic and e
Autor:
Yann Joly, David Bujold, Charles Dupras, Stephan Beck, Stephanie O.M. Dyke, Guillaume Bourque, Katie M. Saulnier
Publikováno v:
Scientific Data
Scientific Data, Vol 6, Iss 1, Pp 1-6 (2019)
Scientific Data, Vol 6, Iss 1, Pp 1-6 (2019)
In the past decade, there has been a surge in the number of sensitive human genomic and health datasets available to researchers via Data Access Agreements (DAAs) and managed by Data Access Committees (DACs). As this form of sharing increases, so do
Publikováno v:
Medical Law International. 18:219-240
As scientific understanding of the heritable aspects of cancer deepens, the need to effectively communicate genetic information within the families of cancer patients becomes more acute. In the palliative care context, the question of when and how to
Publikováno v:
FACETS, Vol 1, Pp 138-147 (2016)
Facets (Ottawa)
Facets (Ottawa)
In setting up a data access policy to share controlled access data from the McGill Epigenomics Mapping Centre (EMC), an International Human Epigenome Consortium (IHEC) partner project, we encountered ethical and legal challenges that are likely to be